產(chǎn)品展示
Vimentin波形蛋白(抗原)
點(diǎn)擊次數(shù):15發(fā)布時(shí)間:2016/7/24 15:40:45

更新日期:2016/7/24 15:40:45
所 在 地:中國(guó)大陸
產(chǎn)品型號(hào):
優(yōu)質(zhì)供應(yīng)
詳細(xì)內(nèi)容
【Vimentin波形蛋白(抗原)】齊一生物科技(上海)有限公司專(zhuān)業(yè)經(jīng)營(yíng)高效液相色譜法、可見(jiàn)分光光度法、紫外分光光度法、酶標(biāo)法檢測(cè)試劑盒齊一生物銷(xiāo)售:021-6034 8496;181214 53965;173021 04490【Vimentin波形蛋白(抗原)】
6000-5000 Specimen Collection Tubes CNY 【Vimentin波形蛋白(抗原)】
5000-1430 MST Vortexer II - FoamFeetAssembly, 110V CNY
5128-1220 Specimen Transport Medium (STM) CE CNY
5123-1220 Female Swab Specimen Collection KitTM CNY
5100-1400IVD hc2 Sample Conversion Kit CNY
EA11424 EASYartus BKV RG_II CNY
5050-1075 V.1 CD Rom Manual, MST Vortexer 2 CNY
EA10124 EASYartus EBV RG PCR Kit 2 CNY
BR-02 DxS B-RAF Mutation Test Kit CNY
9240729 Tubing, 3/8"OD , Red, AP CNY
9240719 Cable Carrier, Capper, Elevator, AP CNY
9240701 O-Ring, Shaker, Lower Body, AP96/196 CNY
9240696 Fitting, Barbed, 1/4" ID tube, AP CNY
9243651 Comprehen Valid., QIAgility """The Comprehensive Validation Support plan specific to a laboratory's needs will incorporate all of the requirements for the internal validation guidelines from the FBI's Quality Assurance Standards (QAS).
The Comprehensive Validation Support service includes all travel and labor charges for up to 20 days by the QIAGEN Validation Team. Typically, one week will be required to extract, quantify, and amplify the validation study samples and may require multiple individuals. Usually, two weeks is required to analyze the data and one week to write the final report. The expected time period to complete the Comprehensive Validation is six weeks. The actual time may vary depending on resource availability, including laboratory time dedicated to validation activities.
Lab Work – The QIAGEN specialist(s) will travel to the laboratory to conduct the on-site validation lab work. The QIAGEN specialist team will perform and complete all extractions, quantifications, amplfications, and capillary electrophoresis. The laboratory is responsible for providing systems/protocols that may be needed (generally laboratory SOPs, ex. interpretation guidelines). Additionally, the laboratory staff may be required to provide additional data needed for interpretation (ex. quantification/amplification/CE results) during the data review phase of the validation.
Once the final scope of the validation is determined, QIAGEN will provide a quote for all consumables required for the validation. Non-QIAGEN chemistry and accessories are not included and should be purchased to cover the validation experimental design including qPCR, STR, NIST standards, required samples types (blood, semen, buccal samples) and required substrates (swabs, materials, etc). For planning purposes and to ensure a smooth process, the Customer is expected to have all materials on-hand and inventoried one (1) week prior to the validation start date.
Data Analysis – The Comprehensive Validation Support plan encompasses data collection (quants, amps, CE) during the on-site visit. The laboratory may be responsible for sharing (typically electronically via e-mail) any validation data requested after the on-site visit. A QIAGEN specialist will complete all of the data analysis produced from the validation study design. This includes qPCR (quant) and STR (amp) analysis and linkage to starting samples.
Validation data CD/flashdrive – QIAGEN will review the validation data and draft a validation summary document, ensuring compliance with the FBI's QAS requirements/standards. QIAGEN will send validation data in an electronic format (email/CD/flashdrive) to the laboratory. The laboratory is responsible for final compilation, any format change preferences, review and signoff of the validation report. The documentation provided by QIAGEN will aide in demonstrating compliance with all accreditation guidelines during laboratory audits. Should a hard copy of the validation study be preferred, the laboratory is required to specify prior to the onset of the validation.
Post-validation QIAGEN-to-Laboratory Transfer – Following completion of the validation and generation of the draft validation summary document, a designated member of the QIAGEN validation team will review the validation with the Lab Manager and the Technical Leader. Following sign off on the validation report, training of the laboratory DNA staff will occur. Refer to the Post-validation Competency Training for additional information. """ CNY
218076 miScript SYBR Green PCR Kit (2000) CNY
271906 cattletype Milk Prep Kit (50) CNY
289980 intype IC-DNA (1ml) CNY 【Vimentin波形蛋白(抗原)】
280437 virotype BTV RT-PCR Kit (480) CNY
932836 #QIAsymphony Ni-NTA Denat. Kit (384) CNY
800511 Verification Sequencing / DNA production CNY
9238243 ZLV BioRobot M96 User Manual CNY
9019988 ZLV Mainboard, QGY CNY
9020553 Foam angle, transport box, QIAC CNY
9020582 X-Motor, DML3000 CNY
9020584 Y-Belt, DML3000 320 Teeth CNY
9020594 Enclosure, DML3000 CNY
9021006 Motor, Pipettor Y, DCU CNY
9236333 Sample Loop CNY
9013382 Shaker adapter, microplate, LHS CNY
9013275 Motor, gripper, handler T/L, BR3000 CNY
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QYS-03254 血鈣濃度測(cè)試盒 100管/96樣 酶標(biāo)法
QYS-03255 血清鐵濃度測(cè)試盒 50管/48樣 可見(jiàn)分光光度法
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QYS-03257 血鎂濃度測(cè)試盒 50管/48樣 可見(jiàn)分光光度法 【Vimentin波形蛋白(抗原)】
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QYS-03272 土壤汞S-Hg濃度測(cè)試盒 50管/48樣 可見(jiàn)分光光度法
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